1. MG-123 Exonic and intronic NRXN1 deletions: Novel genotype-phenotype correlations. (4th December 2015) Authors: Lowther, Chelsea; Speevak, Marsha; Armour, Christine; Goh, Elaine; Graham, Gail; Li, Chumei; Zeesman, Susan; Nowaczyk, Malgorzata JM; Schultz, Lee-Anne; Morra, Antonella; Nicolson, Robert; Rajguru, Manjulata; Goobie, Sharan; Tarnopolsky, Mark A; Prasad, Chitra; Dick, Paul T; Hussain, Asmaa S; Gaz... Journal: Journal of medical genetics Issue: Volume 52(2015)Supplement 2 Page Start: A9 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. MG-121 Complexity of phenotypes of females with unbalanced x-autosomal translocations exemplified by a case with 46, x, der (x)t (x;16)(p11.2;p13.2) karyotype. (4th December 2015) Authors: Grafodatskaya, Daria; Dell, Edith; Li, Chumei; McCready, Elizabeth Journal: Journal of medical genetics Issue: Volume 52(2015)Supplement 2 Page Start: A8 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. The spectrum of epilepsy in children with 15q13.3 microdeletion syndrome. (November 2021) Authors: Whitney, Robyn; Nair, Arjun; McCready, Elizabeth; Keller, Anne E.; Adil, Ishita Siddiq; Aziz, Aly Shah; Borys, Oksana; Siu, Kaitlyn; Shah, Chintan; Meaney, Brandon F.; Jones, Kevin; RamachandranNair, Rajesh Journal: Seizure Issue: Volume 92(2021) Page Start: 221 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Practice guidelines for BRCA1/2 tumour testing in ovarian cancer. Issue 8 (7th April 2022) Authors: Grafodatskaya, Daria; O'Rielly, Darren D; Bedard, Karine; Butcher, Darci T; Howlett, Christopher J; Lytwyn, Alice; McCready, Elizabeth; Parboosingh, Jillian; Spriggs, Elizabeth L; Vaags, Andrea K; Stockley, Tracy L Journal: Journal of medical genetics Issue: Volume 59:Issue 8(2022) Page Start: 727 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. CCMG practice guideline: laboratory guidelines for next-generation sequencing. Issue 12 (12th July 2019) Authors: Hume, Stacey; Nelson, Tanya N; Speevak, Marsha; McCready, Elizabeth; Agatep, Ron; Feilotter, Harriet; Parboosingh, Jillian; Stavropoulos, Dimitri J; Taylor, Sherryl; Stockley, Tracy L Journal: Journal of medical genetics Issue: Volume 56:Issue 12(2019) Page Start: 792 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Practice patterns of prenatal and perinatal testing in Canadian cytogenetics laboratories. (25th April 2021) Authors: Ashfield, Tamara; McCready, Elizabeth; Shago, Mary; Wang, Hong; Sinclair‐Bourque, Elizabeth; Cappa, Eva; Piche Marolt, Amanda; Chun, Kathy Journal: Prenatal diagnosis Issue: Volume 41:Number 7(2021) Page Start: 843 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Changes in expression of the CD200 tolerance‐signaling molecule and its receptor (CD200R) by villus trophoblasts during first trimester missed abortion and in chronic histiocytic intervillositis. (22nd March 2017) Authors: Clark, David A.; Dmetrichuk, Jennifer M.; McCready, Elizabeth; Dhesy‐Thind, Sukhbinder; Arredondo, Jorge L. Journal: American journal of reproductive immunology Issue: Volume 78:Number 1(2017) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Prader–Willi syndrome and Tay–Sachs disease in association with mixed maternal uniparental isodisomy and heterodisomy 15 in a girl who also had isochromosome Xq. (6th October 2014) Authors: Zeesman, Susan; McCready, Elizabeth; Sadikovic, Bekim; Nowaczyk, Małgorzata JM Journal: American journal of medical genetics Issue: Volume 167:Number 1(2015:Jan.) Page Start: 180 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Further characterization of the 9q31 microdeletion phenotype; delineation of a common region of overlap containing ZNF462. Issue 3 (3rd December 2022) Authors: Brady, Lauren; Ballantyne, Mark; Duck, John; Fisker, Thomas; Kleefman, Ryan; Li, Chumei; Nfonsam, Landry; Schultz, Lee‐Anne; Tarnopolsky, Mark; McCready, Elizabeth Journal: Molecular genetics & genomic medicine Issue: Volume 11:Issue 3(2023) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Partial monosomy 1q43 and partial trisomy 20q13.2: a case report. Issue 3 (July 2016) Authors: Ho, Boey S.; McCready, Elizabeth; Nowaczyk, Malgorzata J.M. Journal: Clinical dysmorphology Issue: Volume 25:Issue 3(2016:Jul.) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗